Chemistry In Focus
7th Edition
ISBN: 9781337399692
Author: Tro, Nivaldo J.
Publisher: Cengage Learning,
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Chapter 5, Problem 3SC
Interpretation Introduction
Interpretation:
A Lewis structure for a molecule in which the central atom lacks an octet is to be explained.
Concept introduction:
In Lewis structures, dots are used to represent the valence electrons.
Structures with octets (eight dots) or duets (two dots) are stable configurations.
The atoms in a molecule are linked together with each other through
Atoms can share more than one electron pair to form a complete octet resulting in multiple bonds.
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What does the phrase 'fit for purpose' mean in relation to analytical chemistry? Please provide examples too.
For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the
benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene.
Molecule
Inductive Effects
Resonance Effects
Overall Electron-Density
×
NO2
○ donating
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O withdrawing
O withdrawing
O electron-rich
electron-deficient
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E
[
CI
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withdrawing
O no inductive effects
Explanation
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○ donating
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no resonance effects
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electron-deficient
O similar to benzene
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Understanding how substituents activate
Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic
aromatic substitution.
Explanation
HN
NH2
Check
X
(Choose one)
(Choose one)
(Choose one)
(Choose one)
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Chapter 5 Solutions
Chemistry In Focus
Ch. 5 - Drawing Lewis Structures for Ionic Compounds Draw...Ch. 5 - Using Lewis Structures to Determine the Correct...Ch. 5 - Prob. 5.3YTCh. 5 - Prob. 5.4YTCh. 5 - Drawing Lewis Structures for Covalent Compounds...Ch. 5 - Prob. 5.6YTCh. 5 - Prob. 5.7YTCh. 5 - Prob. 5.8YTCh. 5 - Prob. 5.9YTCh. 5 - Determining if a Molecule Is Polar Is SCl2 a polar...
Ch. 5 - Based on the Lewis structures for hydrogen and...Ch. 5 - Prob. 2SCCh. 5 - Prob. 3SCCh. 5 - Prob. 4SCCh. 5 - Which one of the following bonds is polar? a. a...Ch. 5 - Prob. 6SCCh. 5 - Why is salt, NaCl, relatively harmless even though...Ch. 5 - If sodium is dropped into water, a loud fizzing...Ch. 5 - Explain ionic bonding according to Lewis theory.Ch. 5 - Prob. 4ECh. 5 - Prob. 5ECh. 5 - Prob. 6ECh. 5 - Draw electron dot structures for the following...Ch. 5 - Explain VSEPR theory. According to this theory,...Ch. 5 - Prob. 9ECh. 5 - Prob. 10ECh. 5 - In what ways is water unique? What about the water...Ch. 5 - What is the difference between a polar and a...Ch. 5 - Why do polar molecules have a greater tendency to...Ch. 5 - Prob. 14ECh. 5 - Lewis Structures for Atoms Draw Lewis structures...Ch. 5 - Draw Lewis structures for each of the following...Ch. 5 - Ionic Lewis Structures Draw a Lewis structure for...Ch. 5 - Draw a Lewis structure for each of the following...Ch. 5 - Draw a Lewis structure for each of the following...Ch. 5 - Draw a Lewis structure for each of the following...Ch. 5 - Covalent Lewis Structures Draw a Lewis structure...Ch. 5 - Draw a Lewis structure for each molecular...Ch. 5 - General Lewis Structures Determine whether each...Ch. 5 - Determine whether each compound is ionic or...Ch. 5 - What is wrong with each Lewis structure? Fix the...Ch. 5 - What is wrong with each Lewis structure? Fix the...Ch. 5 - Predicting the Shapes of Molecules Use VSEPR...Ch. 5 - Use VSEPR theory to determine the geometry of the...Ch. 5 - Draw a Lewis structure and use VSEPR theory to...Ch. 5 - Draw a Lewis structure and use VSEPR theory to...Ch. 5 - CF2Cl2 is a chlorofluorocarbon implicated in ozone...Ch. 5 - Chlorofluorocarbons have been banned because they...Ch. 5 - Determining Molecular Polarity Determine whether...Ch. 5 - Determine whether each molecule is polar:...Ch. 5 - Determine whether each molecule is polar:...Ch. 5 - Determine whether each molecule is polar:...Ch. 5 - Explain why water would be a gas at room...Ch. 5 - Prob. 38ECh. 5 - Prob. 39ECh. 5 - One of the observations that led G. N. Lewis to...Ch. 5 - G. N. Lewis developed a model for chemical bonding...Ch. 5 - The opening quote of this chapter states that Man...Ch. 5 - Draw a Lewis structure of the H2 molecule. If you...Ch. 5 - Prob. 44ECh. 5 - The Lewis structures for CH4,N2,andCO2, along with...Ch. 5 - CH3COCH3 (acetone) is a common laboratory solvent...
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- Identifying electron-donating and electron-withdrawing effects on benzene For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Inductive Effects Resonance Effects Overall Electron-Density Molecule CF3 O donating O donating O withdrawing O withdrawing O no inductive effects O no resonance effects electron-rich electron-deficient O similar to benzene CH3 O donating O withdrawing O no inductive effects O donating O withdrawing Ono resonance effects O electron-rich O electron-deficient O similar to benzene Explanation Check Х © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Centerarrow_forward* Hint: Think back to Chem 1 solubility rules. Follow Up Questions for Part B 12. What impact do the following disturbances to a system at equilibrium have on k, the rate constant for the forward reaction? Explain. (4 pts) a) Changing the concentration of a reactant or product. (2 pts) b) Changing the temperature of an exothermic reaction. (2 pts) ofarrow_forwardDraw TWO general chemical equation to prepare Symmetrical and non-Symmetrical ethers Draw 1 chemical reaction of an etherarrow_forward
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- Rank each of the following substituted benzene molecules in order of which will react fastest (1) to slowest (4) by electrophilic aromatic substitution. OCH 3 (Choose one) OH (Choose one) Br (Choose one) Explanation Check NO2 (Choose one) © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Aarrow_forwardFor each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects O donating O withdrawing O no inductive effects Resonance Effects Overall Electron-Density ○ donating ○ withdrawing O no resonance effects O electron-rich O electron-deficient O similar to benzene Cl O donating O withdrawing ○ donating ○ withdrawing O no inductive effects O no resonance effects O Explanation Check O electron-rich O electron-deficient similar to benzene X © 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessarrow_forwardIdentifying electron-donating and For each of the substituted benzene molecules below, determine the inductive and resonance effects the substituent will have on the benzene ring, as well as the overall electron-density of the ring compared to unsubstituted benzene. Molecule Inductive Effects NH2 ○ donating NO2 Explanation Check withdrawing no inductive effects Resonance Effects Overall Electron-Density ○ donating O withdrawing O no resonance effects O donating O withdrawing O donating withdrawing O no inductive effects Ono resonance effects O electron-rich electron-deficient O similar to benzene O electron-rich O electron-deficient O similar to benzene olo 18 Ar 2025 McGraw Hill LLC. All Rights Reserved. Terms of Use | Privacy Center | Accessibilityarrow_forward
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